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Cytoxan
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Help!
Brain scans are negative and they are continuing to give her prednisone and
cytoxan
for Wegners. I am so relieved she was found but she is still having problems with her memory. The doctors don't seem to think it is from her meds. Any help would be appreciated. Memory loss experiences?
Brain scans are negative and they are continuing to give her prednisone and
cytoxan
for Wegners. I am so relieved she was found but she is still having problems with her memory. The doctors don't seem to think it is from her meds. Any help would be appreciated. Memory loss experiences?
Deedrah
in
Vasculitis UK
7 years ago
Seeking Surgery & Chemo Advice Please
Because I was treated with andriamycin for soft tissue sarcoma six years ago, my chemo will instead likely be Taxotere/
Cytoxan
. Any helpful advice for me for the surgical experience? Has anyone had this type of chemo and can share with me their side effects experience?
Because I was treated with andriamycin for soft tissue sarcoma six years ago, my chemo will instead likely be Taxotere/
Cytoxan
. Any helpful advice for me for the surgical experience? Has anyone had this type of chemo and can share with me their side effects experience?
Tinydancer1
in
SHARE Breast Cancer Support
7 years ago
Unstable INR, Rashing Accompanying Migraines, and Hematologist considering Rituxan or Cytoxan- Reasonable?
Question: the hematologist who is investigating my son is suggesting suppressing the immune system with either Rituxan or
cytoxan
? He thinks Rituxan. (He saw my rash yesterday when I brought my son in for testing and was shocked at my rash.
Question: the hematologist who is investigating my son is suggesting suppressing the immune system with either Rituxan or
cytoxan
? He thinks Rituxan. (He saw my rash yesterday when I brought my son in for testing and was shocked at my rash.
KellyInTexas
Administrator
in
Hughes Syndrome APS Forum
7 years ago
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Chemo
I will have Taxotere and
Cytoxan
. I'm not sure I'm spelling them correctly. Also anyone have experience with the Penguin Cold Cap to keep your hair? Any advice appreciated
I will have Taxotere and
Cytoxan
. I'm not sure I'm spelling them correctly. Also anyone have experience with the Penguin Cold Cap to keep your hair? Any advice appreciated
Honeyto7
in
SHARE Breast Cancer Support
7 years ago
PF and PAN
I appear to have contracted PF from taking
cytoxan
while fighting PAN some 15 years ago. this is all new to me.
I appear to have contracted PF from taking
cytoxan
while fighting PAN some 15 years ago. this is all new to me.
ronc
in
Lung Conditions Community Forum
7 years ago
Taxotere and Cytoxan chemotherapy drug information.
I am interested in anyone that has had the chemotherapy drugs Taxotere and
Cytoxan
. I start my first chemotherapy regime tomorrow morning with this chemotherapy. Thank you in advance.
I am interested in anyone that has had the chemotherapy drugs Taxotere and
Cytoxan
. I start my first chemotherapy regime tomorrow morning with this chemotherapy. Thank you in advance.
Imat
in
SHARE Breast Cancer Support
7 years ago
Cancer History
At 44, had a left breast lumpectomy (no lymph node involvement, Stage I) followed by 6 rounds of adriamycin/
cytoxan
, 5 years of tamoxifen.
At 44, had a left breast lumpectomy (no lymph node involvement, Stage I) followed by 6 rounds of adriamycin/
cytoxan
, 5 years of tamoxifen.
miyoshi
in
SHARE Ovarian Cancer Support
7 years ago
POTS? Is it possible...
I'm doing
Cytoxan
infusions right now, and they're working on the Behcet's slowly. I just don't know if this is POTS and if it's related to the Behcet's, and what it means treatment wise.
I'm doing
Cytoxan
infusions right now, and they're working on the Behcet's slowly. I just don't know if this is POTS and if it's related to the Behcet's, and what it means treatment wise.
NerdyChristina
in
Behçet's UK
7 years ago
Triple Negative survival!!!!
I have had a lumpectomy, 4 rounds of Adiamycin, and 4 rounds of
Cytoxan
/Taxol, double mastectomy, and 33 rounds of radiation. They found out before I started chemo that my cancer was metastatic in three of my lymph nodes, but they were not under my arms.
I have had a lumpectomy, 4 rounds of Adiamycin, and 4 rounds of
Cytoxan
/Taxol, double mastectomy, and 33 rounds of radiation. They found out before I started chemo that my cancer was metastatic in three of my lymph nodes, but they were not under my arms.
stressedx3
in
SHARE Metastatic Breast Cancer
8 years ago
New Treatments
In addition to the standard chemo-immunotherapy combinations of the past (These are regimens like Fludarabine-
Cytoxan
-Rituxan and Bendamustine-Rituxan) there are also newer anti-CD20 monoclonal antibodies with a drug called Gazyva (obinutuzumab).
In addition to the standard chemo-immunotherapy combinations of the past (These are regimens like Fludarabine-
Cytoxan
-Rituxan and Bendamustine-Rituxan) there are also newer anti-CD20 monoclonal antibodies with a drug called Gazyva (obinutuzumab).
Jemisavs5
in
CLL Support
8 years ago
Still in treatment since August 2015. Any advise?
I had (1) Doxil single agent (2) carbo/gemzar (3) gemzar/
Cytoxan
and carbo/taxol. I had to stop due to severe allergy to taxol.. That was in July 2016. . I tried getting into another hospital.
I had (1) Doxil single agent (2) carbo/gemzar (3) gemzar/
Cytoxan
and carbo/taxol. I had to stop due to severe allergy to taxol.. That was in July 2016. . I tried getting into another hospital.
GreenSnow
in
My Ovacome
8 years ago
2nd recurrence. 4 chemo combos all failed. Any suggestions?
Quite devastated and still wanting to fight more I consulted another Oncologist who suggested adding IV cyclophosphamide (
Cytoxan
) to gemzar. But it got worse as the CA125 kept doubling instead. Now I am not even stable. With a CA 125 of 263 I started on carbo /taxol.
Quite devastated and still wanting to fight more I consulted another Oncologist who suggested adding IV cyclophosphamide (
Cytoxan
) to gemzar. But it got worse as the CA125 kept doubling instead. Now I am not even stable. With a CA 125 of 263 I started on carbo /taxol.
GreenSnow
in
My Ovacome
8 years ago
Chemotherapy for Lupus Nephritis
I am currently doing the euro lupus regime (6 fortnightly doses of 500mgs of
cytoxan
). I have completed 3 doses which I am thankful that I handle well. However the protein in my urine has not started to come down yet and I am getting worried that it won't work!
I am currently doing the euro lupus regime (6 fortnightly doses of 500mgs of
cytoxan
). I have completed 3 doses which I am thankful that I handle well. However the protein in my urine has not started to come down yet and I am getting worried that it won't work!
Lilly25
in
LUPUS UK
8 years ago
My treatments
So my treatments are
cytoxan
/adriamycin every 2 weeks x4 treatments (#3 will be tomorrow). This will be followed by 12 weekly taxol treatments. Also have neulasta auto injector every session. So far I have lost 90% of my hair on my head. Eyebrows still good.
So my treatments are
cytoxan
/adriamycin every 2 weeks x4 treatments (#3 will be tomorrow). This will be followed by 12 weekly taxol treatments. Also have neulasta auto injector every session. So far I have lost 90% of my hair on my head. Eyebrows still good.
CancerkickerKathy
in
My Breast Cancer Community
8 years ago
Weight gain and hair loss
I will be getting the red death(devil)
cytoxan
and adriamycin every 2 weeks x 4 treatments. Then taxol every week for 12 weeks. I know my hair will fall out but what about facial hair? Eyebrows? Legs? I sure hope that it won't come in curly. I don't need a curly mustache lol.
I will be getting the red death(devil)
cytoxan
and adriamycin every 2 weeks x 4 treatments. Then taxol every week for 12 weeks. I know my hair will fall out but what about facial hair? Eyebrows? Legs? I sure hope that it won't come in curly. I don't need a curly mustache lol.
CancerkickerKathy
in
My Breast Cancer Community
9 years ago
Has anyone had eight months of treatment using Rituxan and Treanda (bendamustine)
In July 2008 began treatment using Rituxan and
Cytoxan
. Had 4 treatments from July 2008 to October 2008. WBC started climbing again in July 2009. Back to W&W. In March 2011 started treatment using Rixtuan and Treanda. Had 6 treatments from March 2011 to August 2011.
In July 2008 began treatment using Rituxan and
Cytoxan
. Had 4 treatments from July 2008 to October 2008. WBC started climbing again in July 2009. Back to W&W. In March 2011 started treatment using Rixtuan and Treanda. Had 6 treatments from March 2011 to August 2011.
Janetfld
in
CLL Support
9 years ago
Recommendation and your views please ..........................................................
Have looked at other med's Cellcept,
Cytoxan
, Imuran, lefunomide etc but would really appreciate your views and opinions. I really do not want to have another course of steroids they make me feel poorly, so want to go to my Rheumy with something else in mind. Thank you for your advice xx
Have looked at other med's Cellcept,
Cytoxan
, Imuran, lefunomide etc but would really appreciate your views and opinions. I really do not want to have another course of steroids they make me feel poorly, so want to go to my Rheumy with something else in mind. Thank you for your advice xx
beckybooboo
in
LUPUS UK
11 years ago
umbilical stem cell treatment
They put me on
cytoxan
, prenisone, cholcine, Immuran. On my own I decided to get off the immuno suppresive therapy. I started learning about my disease and how it effects my body. I learned alot and decided that stem cells was the way to go.
They put me on
cytoxan
, prenisone, cholcine, Immuran. On my own I decided to get off the immuno suppresive therapy. I started learning about my disease and how it effects my body. I learned alot and decided that stem cells was the way to go.
tamirra
in
Behçet's UK
11 years ago
Rituximab poss. next drug. What to ask the Dr.? Apt in three days.
Was treated with
cytoxan
and high doses of prednisione for 6 months. Since that time, I have not had an effective RA drug. Any thoughts would be welcome. Thx. Umamel
Was treated with
cytoxan
and high doses of prednisione for 6 months. Since that time, I have not had an effective RA drug. Any thoughts would be welcome. Thx. Umamel
umamel
in
NRAS
12 years ago
Dad diagnosed with Wegener's Granulomatosis
Now on therapy with prednisone (50mg per day and cutting down 5 mg every week) and a monthly dose of cyclophosphamide (I believe called
Cytoxan
). Any help on how to understand what he is going through and support him both mentally and physically would be very appreciated.
Now on therapy with prednisone (50mg per day and cutting down 5 mg every week) and a monthly dose of cyclophosphamide (I believe called
Cytoxan
). Any help on how to understand what he is going through and support him both mentally and physically would be very appreciated.
zmajevi
in
Vasculitis UK
12 years ago
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